Life Rising Brain ECM Dietary Supplement Contains Lead - Recall
Life Rising Corp recalls Brain ECM dietary supplement due to lead contamination. The product contains lead, a harmful substance that can cause health issues. Consumers should stop using the product immediately.
Stop using this now
The dietary supplement Brain ECM contains lead.
Contact the company
What happened, in plain English
Life Rising Corp recalls its Brain ECM dietary supplement because it contains lead. This poses a health risk, especially for children and pregnant women, as lead exposure can cause serious health problems. Read more at govinfonow.com/recall/23209-life-rising-brain-ecm-dietary-supplement-contains-lead-recall.
Source Summary by GovInfoNow · govinfonow.com/recall/23209-life-rising-brain-ecm-dietary-supplement-contains-lead-recall · Updated October 9, 2026 · FDA enforcement record: FDA #F-1624-2017
Cite this page
“Life Rising Brain ECM Dietary Supplement Contains Lead - Recall.” GovInfoNow, updated October 9, 2026. https://govinfonow.com/recall/23209-life-rising-brain-ecm-dietary-supplement-contains-lead-recall. Based on FDA recall #F-1624-2017 (https://api.fda.gov/food/enforcement.json?search=recall_number:%22F-1624-2017%22&limit=1).
Why it’s dangerous
The Brain ECM supplement contains lead, a toxic heavy metal. Lead exposure can cause serious health issues, including developmental problems in children and neurological damage in adults.
Who’s affected
Anyone who owns or uses the Brain ECM supplement. Children and pregnant women are at higher risk due to lead exposure.
How to tell if you have this one
Look for the product in white plastic bottles with green lettering. The label includes 'LIFE RISING, Chinese Herbal Supplement, BRAIN- ECM, Brain E-Calm, 54 Capsules'.
- Brand
Life Rising- Category
Food
What to do — step by step
Stop Using It Now
Immediately stop using the Brain ECM supplement as it contains lead, which can cause serious health issues.
Where it went and when
Where it was distributed
Distributed in Arkansas and Illinois, and outside the U.S.
FDA distribution: “IL; AR. Product was not shipped to foreign consignees.” States read from FDA’s own wording; “not listed” means the notice does not name it.
States: Arkansas, Illinois.
Recall timeline
FDA terminated this recall 2.5 years after the firm started it.
- Firm started the recall
- FDA classified it Class I
- Published in FDA’s Enforcement Report
- FDA terminated the recall
Dates from the agency record only; steps without a date are left out.
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Where this comes from
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
- Official source: FDA Recall #F-1624-2017 (September 14, 2016) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for F-1624-2017 to see it in context.
- Plain-language summary written by qwen3:4b on October 9, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
- GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.